检索结果 - Radmanesh, Farid

Translational Genomics in Neurocritical Care: a Review 由 Myserlis, Pavlos, Radmanesh, Farid, Anderson, Christopher D.

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Congenital spinal tumor in a patient with encephalocele and hydrocephalus: a case report 由 Radmanesh, Farid, Nejat, Farideh, Mahjoub, Fatemeh, El Khashab, Mostafa

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Severe cerebral involvement in adult-onset hemophagocytic lymphohistiocytosis 由 Radmanesh, Farid, Rodriguez-Pla, Alicia, Pincus, Michael D., Burns, Joseph D.

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Accuracy of imputation to infer unobserved APOE epsilon alleles in genome-wide genotyping data 由 Radmanesh, Farid, Devan, William J, Anderson, Christopher D, Rosand, Jonathan, Falcone, Guido J

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Mutations in LAMB1 Cause Cobblestone Brain Malformation without Muscular or Ocular Abnormalities 由 Radmanesh, Farid, Caglayan, Ahmet Okay, Silhavy, Jennifer L., Yilmaz, Cahide, Cantagrel, Vincent, Omar, Tarek, Rosti, Başak, Kaymakcalan, Hande, Gabriel, Stacey, Li, Mingfeng, Šestan, Nenad, Bilguvar, Kaya, Dobyns, William B., Zaki, Maha S., Gunel, Murat, Gleeson, Joseph G.

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Risk Factors for CT Angiography Spot Sign in Deep and Lobar Intracerebral Hemorrhage are Shared 由 Radmanesh, Farid, Falcone, Guido J., Anderson, Christopher D., Battey, Thomas W. K., Ayres, Alison M., Vashkevich, Anastasia, McNamara, Kristen A., Schwab, Kristin, Romero, Javier M., Viswanathan, Anand, Greenberg, Steven M., Goldstein, Joshua N., Rosand, Jonathan, Brouwers, H. Bart

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Genetic Architecture of White Matter Hyperintensities Differs in Hypertensive and Nonhypertensive Ischemic Stroke 由 Adib-Samii, Poneh, Devan, William, Traylor, Matthew, Lanfranconi, Silvia, Zhang, Cathy R., Cloonan, Lisa, Falcone, Guido J., Radmanesh, Farid, Fitzpatrick, Kaitlin, Kanakis, Allison, Rothwell, Peter M., Sudlow, Cathie, Boncoraglio, Giorgio B., Meschia, James F., Levi, Chris, Dichgans, Martin, Bevan, Steve, Rosand, Jonathan, Rost, Natalia S., Markus, Hugh S.

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A genome-wide association study of outcome from traumatic brain injury 由 Kals, Mart, Kunzmann, Kevin, Parodi, Livia, Radmanesh, Farid, Wilson, Lindsay, Izzy, Saef, Anderson, Christopher D., Puccio, Ava M., Okonkwo, David O., Temkin, Nancy, Steyerberg, Ewout W., Stein, Murray B., Manley, Geoff T., Maas, Andrew I.R., Richardson, Sylvia, Diaz-Arrastia, Ramon, Palotie, Aarno, Ripatti, Samuli, Rosand, Jonathan, Menon, David K.

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Association of Traumatic Brain Injury With the Risk of Developing Chronic Cardiovascular, Endocrine, Neurological, and Psychiatric Disorders 由 Izzy, Saef, Chen, Patrick M., Tahir, Zabreen, Grashow, Rachel, Radmanesh, Farid, Cote, David J., Yahya, Taha, Dhand, Amar, Taylor, Herman, Shih, Shirley L., Albastaki, Omar, Rovito, Craig, Snider, Samuel B., Whalen, Michael, Nathan, David M., Miller, Karen K., Speizer, Frank E., Baggish, Aaron, Weisskopf, Marc G., Zafonte, Ross

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Rare Coding Variation and Risk of Intracerebral Hemorrhage 由 Radmanesh, Farid, Falcone, Guido J., Anderson, Christopher D., McWilliams, David, Devan, William J., Brown, W Mark, Battey, Thomas W. K., Ayres, Alison M., Raffeld, Miriam R., Schwab, Kristin, Sun, Guangyun, Deka, Ranjan, Viswanathan, Anand, Goldstein, Joshua N., Greenberg, Steven M., Tirschwell, David L., Silliman, Scott L., Selim, Magdy, Meschia, James F., Brown, Devin L., Worrall, Bradford B., Langefeld, Carl D., Woo, Daniel, Rosand, Jonathan

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COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls 由 Rannikmäe, Kristiina, Sivakumaran, Vhinoth, Millar, Henry, Malik, Rainer, Anderson, Christopher D., Chong, Mike, Dave, Tushar, Falcone, Guido J., Fernandez-Cadenas, Israel, Jimenez-Conde, Jordi, Lindgren, Arne, Montaner, Joan, O'Donnell, Martin, Paré, Guillaume, Radmanesh, Farid, Rost, Natalia S., Slowik, Agnieszka, Söderholm, Martin, Traylor, Matthew, Pulit, Sara L., Seshadri, Sudha, Worrall, Brad B., Woo, Daniel, Markus, Hugh S., Mitchell, Braxton D., Dichgans, Martin, Rosand, Jonathan, Sudlow, Cathie L.M.

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Genome-Wide Association Study (GWAS) and Genome-Wide Environment Interaction Study (GWEIS) of Depressive Symptoms in African American and Hispanic/Latina Women 由 Dunn, Erin C., Wiste, Anna, Radmanesh, Farid, Almli, Lynn M., Gogarten, Stephanie M., Sofer, Tamar, Faul, Jessica D., Kardia, Sharon L.R., Smith, Jennifer A., Weir, David R., Zhao, Wei, Soare, Thomas W., Mirza, Saira S., Hek, Karin, Tiemeier, Henning W., Goveas, Joseph S., Sarto, Gloria E., Snively, Beverly M., Cornelis, Marilyn, Koenen, Karestan C., Kraft, Peter, Purcell, Shaun, Ressler, Kerry J., Rosand, Jonathan, Wassertheil-Smoller, Sylvia, Smoller, Jordan W.

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APOE ε variants increase risk of warfarin-related intracerebral hemorrhage 由 Falcone, Guido J., Radmanesh, Farid, Brouwers, H. Bart, Battey, Thomas W.K., Devan, William J., Valant, Valerie, Raffeld, Miriam R., Chitsike, Lennox P., Ayres, Alison M., Schwab, Kristin, Goldstein, Joshua N., Viswanathan, Anand, Greenberg, Steven M., Selim, Magdy, Meschia, James F., Brown, Devin L., Worrall, Bradford B., Silliman, Scott L., Tirschwell, David L., Flaherty, Matthew L., Martini, Sharyl R., Deka, Ranjan, Biffi, Alessandro, Kraft, Peter, Woo, Daniel, Rosand, Jonathan, Anderson, Christopher D.

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17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage 由 Marini, Sandro, Devan, William J., Radmanesh, Farid, Miyares, Laura, Poterba, Timothy, Hansen, Björn M., Norrving, Bo, Jimenez-Conde, Jordi, Giralt-Steinhauer, Eva, Elosua, Roberto, Cuadrado-Godia, Elisa, Soriano, Carolina, Roquer, Jaume, Kourkoulis, Christina E., Ayres, Alison M., Schwab, Kristin, Tirschwell, David L., Selim, Magdy, Brown, Devin L., Silliman, Scott L., Worrall, Bradford B., Meschia, James F., Kidwell, Chelsea S., Montaner, Joan, Fernandez-Cadenas, Israel, Delgado, Pilar, Greenberg, Steven M., Lindgren, Arne, Matouk, Charles, Sheth, Kevin N., Woo, Daniel, Anderson, Christopher D., Rosand, Jonathan, Falcone, Guido J.

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Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease 由 Rannikmäe, Kristiina, Davies, Gail, Thomson, Pippa A., Bevan, Steve, Devan, William J., Falcone, Guido J., Traylor, Matthew, Anderson, Christopher D., Battey, Thomas W.K., Radmanesh, Farid, Deka, Ranjan, Woo, Jessica G., Martin, Lisa J., Jimenez-Conde, Jordi, Selim, Magdy, Brown, Devin L., Silliman, Scott L., Kidwell, Chelsea S., Montaner, Joan, Langefeld, Carl D., Slowik, Agnieszka, Hansen, Björn M., Lindgren, Arne G., Meschia, James F., Fornage, Myriam, Bis, Joshua C., Debette, Stéphanie, Ikram, Mohammad A., Longstreth, Will T., Schmidt, Reinhold, Zhang, Cathy R., Yang, Qiong, Sharma, Pankaj, Kittner, Steven J., Mitchell, Braxton D., Holliday, Elizabeth G., Levi, Christopher R., Attia, John, Rothwell, Peter M., Poole, Deborah L., Boncoraglio, Giorgio B., Psaty, Bruce M., Malik, Rainer, Rost, Natalia, Worrall, Bradford B., Dichgans, Martin, Van Agtmael, Tom, Woo, Daniel, Markus, Hugh S., Seshadri, Sudha, Rosand, Jonathan, Sudlow, Cathie L.M.

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Genetic variants in CETP increase risk of intracerebral hemorrhage 由 Anderson, Christopher D., Falcone, Guido J., Phuah, Chia‐Ling, Radmanesh, Farid, Brouwers, H. Bart, Battey, Thomas W. K., Biffi, Alessandro, Peloso, Gina M., Liu, Dajiang J., Ayres, Alison M., Goldstein, Joshua N., Viswanathan, Anand, Greenberg, Steven M., Selim, Magdy, Meschia, James F., Brown, Devin L., Worrall, Bradford B., Silliman, Scott L., Tirschwell, David L., Flaherty, Matthew L., Kraft, Peter, Jagiella, Jeremiasz M., Schmidt, Helena, Hansen, Björn M., Jimenez‐Conde, Jordi, Giralt‐Steinhauer, Eva, Elosua, Roberto, Cuadrado‐Godia, Elisa, Soriano, Carolina, van Nieuwenhuizen, Koen M., Klijn, Catharina J. M., Rannikmae, Kristiina, Samarasekera, Neshika, Salman, Rustam Al‐Shahi, Sudlow, Catherine L., Deary, Ian J., Morotti, Andrea, Pezzini, Alessandro, Pera, Joanna, Urbanik, Andrzej, Pichler, Alexander, Enzinger, Christian, Norrving, Bo, Montaner, Joan, Fernandez‐Cadenas, Israel, Delgado, Pilar, Roquer, Jaume, Lindgren, Arne, Slowik, Agnieszka, Schmidt, Reinhold, Kidwell, Chelsea S., Kittner, Steven J., Waddy, Salina P., Langefeld, Carl D., Abecasis, Goncalo, Willer, Cristen J., Kathiresan, Sekar, Woo, Daniel, Rosand, Jonathan

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Genetic variation at 16q24.2 is associated with small vessel stroke 由 Traylor, Matthew, Malik, Rainer, Nalls, Mike A., Cotlarciuc, Ioana, Radmanesh, Farid, Thorleifsson, Gudmar, Hanscombe, Ken B., Langefeld, Carl, Saleheen, Danish, Rost, Natalia S., Yet, Idil, Spector, Tim D., Bell, Jordana T., Hannon, Eilis, Mill, Jonathan, Chauhan, Ganesh, Debette, Stephanie, Bis, Joshua C., Longstreth, W.T., Ikram, M. Arfan, Launer, Lenore J., Seshadri, Sudha, Hamilton‐Bruce, Monica Anne, Jimenez‐Conde, Jordi, Cole, John W., Schmidt, Reinhold, Słowik, Agnieszka, Lemmens, Robin, Lindgren, Arne, Melander, Olle, Grewal, Raji P., Sacco, Ralph L., Rundek, Tatjana, Rexrode, Kathryn, Arnett, Donna K., Johnson, Julie A., Benavente, Oscar R., Wasssertheil‐Smoller, Sylvia, Lee, Jin‐Moo, Pulit, Sara L., Wong, Quenna, Rich, Stephen S., de Bakker, Paul I.W., McArdle, Patrick F., Woo, Daniel, Anderson, Christopher D., Xu, Huichun, Heitsch, Laura, Fornage, Myriam, Jern, Christina, Stefansson, Kari, Thorsteinsdottir, Unnur, Gretarsdottir, Solveig, Lewis, Cathryn M., Sharma, Pankaj, Sudlow, Cathie L.M., Rothwell, Peter M., Boncoraglio, Giorgio B., Thijs, Vincent, Levi, Chris, Meschia, James F., Rosand, Jonathan, Kittner, Steven J., Mitchell, Braxton D., Dichgans, Martin, Worrall, Bradford B., Markus, Hugh S.

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Meta-analysis of Genome-wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage 由 Woo, Daniel, Falcone, Guido J., Devan, William J., Brown, W. Mark, Biffi, Alessandro, Howard, Timothy D., Anderson, Christopher D., Brouwers, H. Bart, Valant, Valerie, Battey, Thomas W.K., Radmanesh, Farid, Raffeld, Miriam R., Baedorf-Kassis, Sylvia, Deka, Ranjan, Woo, Jessica G., Martin, Lisa J., Haverbusch, Mary, Moomaw, Charles J., Sun, Guangyun, Broderick, Joseph P., Flaherty, Matthew L., Martini, Sharyl R., Kleindorfer, Dawn O., Kissela, Brett, Comeau, Mary E., Jagiella, Jeremiasz M., Schmidt, Helena, Freudenberger, Paul, Pichler, Alexander, Enzinger, Christian, Hansen, Björn M., Norrving, Bo, Jimenez-Conde, Jordi, Giralt-Steinhauer, Eva, Elosua, Roberto, Cuadrado-Godia, Elisa, Soriano, Carolina, Roquer, Jaume, Kraft, Peter, Ayres, Alison M., Schwab, Kristin, McCauley, Jacob L., Pera, Joanna, Urbanik, Andrzej, Rost, Natalia S., Goldstein, Joshua N., Viswanathan, Anand, Stögerer, Eva-Maria, Tirschwell, David L., Selim, Magdy, Brown, Devin L., Silliman, Scott L., Worrall, Bradford B., Meschia, James F., Kidwell, Chelsea S., Montaner, Joan, Fernandez-Cadenas, Israel, Delgado, Pilar, Malik, Rainer, Dichgans, Martin, Greenberg, Steven M., Rothwell, Peter M., Lindgren, Arne, Slowik, Agnieszka, Schmidt, Reinhold, Langefeld, Carl D., Rosand, Jonathan

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Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval 由 Lin, Honghuang, van Setten, Jessica, Smith, Albert V, Bihlmeyer, Nathan A, Warren, Helen R., Brody, Jennifer A, Radmanesh, Farid, Hall, Leanne, Grarup, Niels, Müller-Nurasyid, Martina, Boutin, Thibaud, Verweij, Niek, Lin, Henry J., Li-Gao, Ruifang, van den Berg, Marten E., Marten, Jonathan, Weiss, Stefan, Prins, Bram, Haessler, Jeffrey, Lyytikäinen, Leo-Pekka, Mei, Hao, Harris, Tamara B., Launer, Lenore J., Li, Man, Alonso, Alvaro, Soliman, Elsayed Z, Connell, John M., Huang, Paul L, Weng, Lu-Chen, Jameson, Heather S, Hucker, William, Hanley, Alan, Tucker, Nathan R, Chen, Yii-Der Ida, Bis, Joshua C., Rice, Kenneth M., Sitlani, Colleen M., Kors, Jan A., Xie, Zhijun, Wen, Chengping, Magnani, Jared W, Nelson, Christopher P, Kanters, Jørgen K., Sinner, Moritz F., Strauch, Konstantin, Peters, Annette, Waldenberger, Melanie, Meitinger, Thomas, Bork-Jensen, Jette, Pedersen, Oluf, Linneberg, Allan, Rudan, Igor, de Boer, Rudolf A., van der meer, Peter, Yao, Jie, Guo, Xiuqing, Taylor, Kent D., Sotoodehnia, Nona, Rotter, Jerome I., Mook-Kanamori, Dennis O., Trompet, Stella, Rivadeneira, Fernando, Uitterlinden, André, Eijgelsheim, Mark, Padmanabhan, Sandosh, Smith, Blair H., Völzke, Henry, Felix, Stephan B., Homuth, Georg, Völker, Uwe, Mangino, Massimo, Spector, Timothy D, Bots, Michiel L., Perez, Marco, Kähönen, Mika, Raitakari, Olli T., Gudnason, Vilmundur, Arking, Dan E, Munroe, Patricia B, Psaty, Bruce M, van Duijn, Cornelia M., Benjamin, Emelia J., Rosand, Jonathan, Samani, Nilesh J, Hansen, Torben, Kääb, Stefan, Polasek, Ozren, van der Harst, Pim, Heckbert, Susan R., Jukema, J. Wouter, Stricker, Bruno H, Hayward, Caroline, Dörr, Marcus, Jamshidi, Yalda, Asselbergs, Folkert W., Kooperberg, Charles, Lehtimäki, Terho, Wilson, James G., Ellinor, Patrick T., Lubitz, Steven A., Isaacs, Aaron

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ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals 由 Bihlmeyer, Nathan A., Brody, Jennifer A., Smith, Albert Vernon, Warren, Helen R., Lin, Honghuang, Isaacs, Aaron, Liu, Ching-Ti, Marten, Jonathan, Radmanesh, Farid, Hall, Leanne M., Grarup, Niels, Mei, Hao, Müller-Nurasyid, Martina, Huffman, Jennifer E., Verweij, Niek, Guo, Xiuqing, Yao, Jie, Li-Gao, Ruifang, van den Berg, Marten, Weiss, Stefan, Prins, Bram P., van Setten, Jessica, Haessler, Jeffrey, Lyytikäinen, Leo-Pekka, Li, Man, Alonso, Alvaro, Soliman, Elsayed Z., Bis, Joshua C., Austin, Tom, Chen, Yii-Der Ida, Psaty, Bruce M., Harrris, Tamara B., Launer, Lenore J., Padmanabhan, Sandosh, Dominiczak, Anna, Huang, Paul L., Xie, Zhijun, Ellinor, Patrick T., Kors, Jan A., Campbell, Archie, Murray, Alison D., Nelson, Christopher P., Tobin, Martin D., Bork-Jensen, Jette, Hansen, Torben, Pedersen, Oluf, Linneberg, Allan, Sinner, Moritz F., Peters, Annette, Waldenberger, Melanie, Meitinger, Thomas, Perz, Siegfried, Kolcic, Ivana, Rudan, Igor, de Boer, Rudolf A., van der Meer, Peter, Lin, Henry J., Taylor, Kent D., de Mutsert, Renée, Trompet, Stella, Jukema, J. Wouter, Maan, Arie C., Stricker, Bruno H.C., Rivadeneira, Fernando, Uitterlinden, André, Völker, Uwe, Homuth, Georg, Völzke, Henry, Felix, Stephan B., Mangino, Massimo, Spector, Timothy D., Bots, Michiel L., Perez, Marco, Raitakari, Olli T., Kähönen, Mika, Mononen, Nina, Gudnason, Vilmundur, Munroe, Patricia B., Lubitz, Steven A., van Duijn, Cornelia M., Newton-Cheh, Christopher H., Hayward, Caroline, Rosand, Jonathan, Samani, Nilesh J., Kanters, Jørgen K., Wilson, James G., Kääb, Stefan, Polasek, Ozren, van der Harst, Pim, Heckbert, Susan R., Rotter, Jerome I., Mook-Kanamori, Dennis O., Eijgelsheim, Mark, Dörr, Marcus, Jamshidi, Yalda, Asselbergs, Folkert W., Kooperberg, Charles, Lehtimäki, Terho, Arking, Dan E., Sotoodehnia, Nona

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